2-Bromo-6-chloro-3-iodo-5-methylpyridine

95%

Reagent Code: #43354
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CAS Number 1822782-03-5

science Other reagents with same CAS 1822782-03-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.36 g/mol
Formula C₆H₄BrClIN
badge Registry Numbers
MDL Number MFCD22572506
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in pharmaceutical research and development. It serves as a key intermediate in the creation of various active pharmaceutical ingredients (APIs), especially those targeting neurological and infectious diseases. Its halogenated structure allows for versatile functionalization, making it valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to construct diverse heterocyclic frameworks. Additionally, it is employed in agrochemical research for developing novel pesticides and herbicides, leveraging its reactivity to introduce specific biological activity. Its use in material science is also notable, particularly in the preparation of advanced organic materials for electronic applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,643.00

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2-Bromo-6-chloro-3-iodo-5-methylpyridine
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This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in pharmaceutical research and development. It serves as a key intermediate in the creation of various active pharmaceutical ingredients (APIs), especially those targeting neurological and infectious diseases. Its halogenated structure allows for versatile functionalization, making it valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to construct diverse heterocyclic framework

This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in pharmaceutical research and development. It serves as a key intermediate in the creation of various active pharmaceutical ingredients (APIs), especially those targeting neurological and infectious diseases. Its halogenated structure allows for versatile functionalization, making it valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to construct diverse heterocyclic frameworks. Additionally, it is employed in agrochemical research for developing novel pesticides and herbicides, leveraging its reactivity to introduce specific biological activity. Its use in material science is also notable, particularly in the preparation of advanced organic materials for electronic applications.

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